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. 2018 Aug 9;20(11):1517–1524. doi: 10.1093/neuonc/noy134

Table 1.

Analyzed key molecular parameters in the glioblastoma cohort

Assessed Molecular Alteration Assessed Number of Patients Patients VLSM
Presenting Alteration (1) Not Presenting Alteration (0) Proportion (%) Presenting Alteration Permutation-Adjusted P-value
MGMT promoter methylation 221 103 118 46.6 0.401
Methylation class1
IDH glioma, subclass high-grade astrocytoma 237 9 228 3.8 0.021
Glioblastoma, IDH wildtype, subclass mesenchymal “mesenchymal” 237 72 165 30.4 0.739
Glioblastoma, IDH wildtype, subclass RTK I “PGFRA 237 36 201 15.2 0.353
Glioblastoma, IDH wildtype, subclass RTK II “classic” 237 108 129 45.6 0.276
Glioblastoma, IDH wildtype, subclass midline “Midline” 237 5 232 2.1 0.197
Diffuse midline glioma H3 K27M mutant 237 5 232 2.1 0.994
Copy number variation
EGFR amplification 237 108 129 45.6 0.325
PDGFRA amplification 237 12 225 5.1 0.762
MDM4 amplification 236 22 214 9.3 0.515
CDK4 amplification 237 174 63 73.4 0.681
PTEN loss 233 186 47 79.8 0.570
TP53 loss 234 19 215 8.1 0.419
CDKN2A loss 237 108 129 45.6 0.747
NF1 loss 233 38 195 16.3 0.722
RB1 loss 233 67 166 28.8 0.148
MYCN amplification 237 5 232 2.1 0.586
TERT gain 232 10 222 4.3 0.289
CDK6 amplification 237 5 232 2.1 0.834
MET amplification 237 7 230 3.0 0.137
CCND2 gain 230 12 218 5.2 0.089
MDM2 amplification 237 14 223 5.9 0.622

Abbreviation: RTK, receptor tyrosine kinase.

Annotations: 1 = detailed explanation of methylation classes available via https://www.molecularneuropathology.org/mnp/classifier/1; accessed August 23, 2018.